Role of Sirtuins in the Pathobiology of Onco-Hematological Diseases: A PROSPERO-Registered Study and In Silico

João Vitor Caetano Goes1,2, Luiz Gustavo Carvalho1,3, Roberta Taiane Germano de Oliveira1,4

  • 1Center for Research and Drug Development (NPDM), Federal University of Ceara, Fortaleza 60020-181, Ceará, Brazil.

Cancers
|October 14, 2022
PubMed

Insights

Sirtuins (SIRTs) influence aging and solid tumors. This study explores SIRTs

Area of Science:

  • * Hematology and Aging Research
  • * Molecular Biology and Cancer Pathogenesis
  • * Bioinformatics and Gene Expression Analysis

Background:

  • * Sirtuins (SIRTs) are key regulators of cellular and organismal aging.
  • * SIRTs' role in solid tumors is established, but their impact on hematopoietic aging and hematological cancers is understudied.
  • * Hematopoietic aging involves system failures that can lead to neoplasms.

Purpose of the Study:

  • * To systematically review and analyze the role of Sirtuins (SIRTs) in the pathogenesis and prognosis of hematological cancers.
  • * To investigate the link between hematopoietic aging, genomic instability, and the development of hematological malignancies.
  • * To highlight the need for further research into SIRT inhibition for cancer treatment.

Main Methods:

  • * Conducted a systematic review (PROSPERO #CRD42022310079).
  • * Performed in silico analysis using the GEPIA database for gene expression.
  • * Synthesized evidence on SIRTs' role in hematological cancer pathobiology.

Main Results:

  • * Sirtuin (SIRT) gene family members are implicated in aging processes.
  • * In silico analysis suggests SIRTs' involvement in the pathobiology of hematological malignancies, including leukemias, lymphomas, and myeloma.
  • * Evidence supports the role of SIRTs in the advancement of pathogenesis and/or prognosis in hematological cancers.

Conclusions:

  • * Sirtuins (SIRTs) are crucial in hematopoietic aging and the development of hematological neoplasms.
  • * Further research and clinical trials are needed to explore SIRT inhibition for controlling clonal progression in hematological cancers.
  • * SIRTs represent promising molecular targets for managing age-related hematopoietic system failures and associated cancers.

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